HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 255959Erstellt: 25. Oktober 2026
Triethylamine → Ethyl 3-diethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate
https://huagongshe.com/reaction/255959
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl 3-(diethylamino)acrylate | HCID 139639 | — |
| Edukt | 2,4-Dichloro-5-fluorobenzoyl chloride | HCID 2736821 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | Ethyl 3-diethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate | HCID 54148103 | 80,2% |
Reaktionsschritte
First 17.1 g of ethyl 3-diethylaminoacrylate are added dropwise and then 10.5 g of triethylamine are added to a solution of 22.75 g of 2,4-dichloro-5-fluorobenzoyl chloride in 80 ml of anhydrous dioxane, while cooling in ice and stirring. The mixture is stirred at room temperature for one hour, heated to boiling under reflux for 45 minutes, and the solvent is removed by distillation in vacuo, and the oily residue is taken up in methylene chloride/water. The phases are separated, and the aqueous solution is again extracted with methylene chloride. The combined organic phases are washed with water, dried with sodium sulphate, and the methylene chloride is removed in vacuo. 29 g of ethyl 3-diethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate are obtained as a brown oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04699992 |
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| Quelldatensatz | uspto-grants-1987_10 |
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| ORD ID | ord-3d3b491826424629a8c5a2f225a8892a |
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| Quellennotiz | uspto-grants-1987_10 |
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